Accurate and reliable high-throughput detection of copy number variation in the human genome

This study describes a new tool for accurate and reliable high-throughput detection of copy number variation in the human genome. We have constructed a large-insert clone DNA microarray covering the entire human genome in tiling path resolution that we have used to identify copy number variation in...

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Bibliografiset tiedot
Päätekijät: Fiegler, Heike, Redon, Richard, Andrews, Dan, Scott, Carol, Andrews, Robert, Carder, Carol, Clark, Richard, Dovey, Oliver, Ellis, Peter, Feuk, Lars, French, Lisa, Hunt, Paul, Kalaitzopoulos, Dimitrios, Larkin, James, Montgomery, Lyndal, Perry, George H., Plumb, Bob W., Porter, Keith, Rigby, Rachel E., Rigler, Diane, Valsesia, Armand, Langford, Cordelia, Humphray, Sean J., Scherer, Stephen W., Lee, Charles, Hurles, Matthew E., Carter, Nigel P.
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: Cold Spring Harbor Laboratory Press 2006
Aiheet:
Methods
Linkit:https://ncbi.nlm.nih.gov/pmc/articles/PMC1665640/
https://ncbi.nlm.nih.gov/pubmed/17122085
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1101/gr.5630906
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